afibrinogenemia

Preferred Label : afibrinogenemia;

MeSH definition : A deficiency or absence of FIBRINOGEN in the blood.;

MeSH synonym : afibrinogenemias;

CISMeF synonym : deficiencies, fibrinogen; deficiency, fibrinogen;

MeSH hyponym : Fibrinogen Deficiencies; Fibrinogen Deficiency;

Related MeSH term : congenital afibrinogenemia; Afibrinogenemia, Congenital; Afibrinogenemias, Congenital; Congenital Afibrinogenemias; Familial Afibrinogenemia; Afibrinogenemia, Familial; Afibrinogenemias, Familial; Familial Afibrinogenemias; Congenital Afibrinogenaemia; Afibrinogenaemia, Congenital; Afibrinogenaemias, Congenital; Congenital Afibrinogenaemias; Hypofibrinogenemia, Congenital; Congenital Hypofibrinogenemia; Congenital Hypofibrinogenemias; Hypofibrinogenemias, Congenital;

MeSH annotation : a blood coag disord;

Wikipedia link : https://en.wikipedia.org/wiki/Congenital afibrinogenemia;

Details

Origin ID

D000347;

UMLS CUI

C0001733;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Afibrinogenemia [PASCAL descriptor]
- Afibrinogenemia, congenital [OMIM Phenotype]
- Congenital afibrinogenemia (disorder) [SNOMED CT concept]
- Congenital hypofibrinogenemia [MedDRA LLT]
- Congenital hypofibrinogenemia (disorder) [SNOMED CT concept]
- FIBRINOGEN PLASMA DECREASED [WHO-ART Preferred Term]
- Familial afibrinogenemia [ORDO Disease]
- Fibrinogen abnormality (disorder) [SNOMED CT concept]
- Fibrinogenopenia [MedDRA LLT]
- Fibrinopenia [MedDRA LLT]
- Hereditary deficiency of other clotting factors [ICD-10 Sub-category]
- Hereditary factor I deficiency disease (disorder) [SNOMED CT concept]
- Hypofibrinogenaemia [MedDRA Preferred Term]
- Hypofibrinogenemia [PASCAL descriptor]
- Hypofibrinogenemia [NCIt concept]
- Hypofibrinogenemia [HPO term]
- Hypofibrinogenemia [MedDRA LLT]
- Hypofibrinogenemia (disorder) [SNOMED CT concept]
- Other specified coagulation defects [ICD-10 Sub-category (who)]
- afibrinogenemia [Blood Transfusion thesaurus concept]
- congenital afibrinogenemia [DO Concept]
- fibrinogen plasma decreased [TUV Concept]
- fibrinogen plasma decreased [TUV Term]
Currated CISMeF NLP mapping
- Afibrinogenaemia [MedDRA LLT]
- Afibrinogenemia [NCIt concept]
- Afibrinogenemia [MedDRA LLT]
- Afibrinogenemia (disorder) [SNOMED CT concept]
- Factor I Deficiency [NCIt concept]
- Fibrinogen deficiency (disorder) [SNOMED CT concept]
- blood clotting factor i deficiency [Disease (Nov.)]
DO Cross reference
- congenital afibrinogenemia [DO Concept]
Indexing information
- fibrinogen merivale [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Congenital fibrinogen deficiency [ORDO Disease]
MeSH Descriptor(s) used for indexing
- fibrinogen [MeSH Descriptor]
Record concept(s)
- Deficiency, Fibrinogen [MeSH concept]
- afibrinogenemia [MeSH concept]
- congenital afibrinogenemia [MeSH concept]
Related MeSH Supplementary Concept(s)
- dysfibrinogenemia, congenital [MeSH Supplementary Concept]
- hypodysfibrinogenemia, congenital [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Afibrinogenaemia [MedDRA LLT]
- Afibrinogenemia [NCIt concept]
- Afibrinogenemia [MedDRA LLT]
- Afibrinogenemia (disorder) [SNOMED CT concept]
- congenital afibrinogenemia [DO Concept]
Validated automatic mappings to BTNT
- congenital fibrinogen deficiency [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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